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Palkovits, M. (1983) · Neuropeptides · doi:10.1016/0143-4179(83)90049-5 · Cited by 28,959

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Paxinos, G., & Watson, C. (1983) · Elsevier eBooks · doi:10.1016/c2009-0-63235-9 · Cited by 28,585

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Kahneman, D. J., Diener, E. F., & Schwarz, N. (1999) · Cited by 7,472

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Berridge, K. C., & Robinson, T. E. (1998) · Brain Research Reviews · doi:10.1016/s0165-0173(98)00019-8 · Cited by 4,127

Untitled work

(1998) · Cited by 4,012

The rat nervous system

Paxinos, G. (1985) · Cited by 3,715

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Gundersen, H. J. G., Bagger, P. V., Bendtsen, T. F., Evans, S. M., Korbo, L., Marcussen, N., Møller, A., Nielsen, K. N., Nyengaard, J. R., Pakkenberg, B., et al. (1988) · Apmis · doi:10.1111/j.1699-0463.1988.tb00954.x · Cited by 2,480

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Berridge, K. C. (1996) · Neuroscience & Biobehavioral Reviews · doi:10.1016/0149-7634(95)00033-b · Cited by 1,901

Inducible and constitutive transcription factors in the mammalian nervous system: control of gene expression by Jun, Fos and Krox, and CREB/ATF proteins

Herdegen, T., & Leah, J. D. (1998) · Brain Research Reviews · doi:10.1016/s0165-0173(98)00018-6 · Cited by 1,369

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Grill, H. J., & Norgren, R. (1978) · Brain Research · doi:10.1016/0006-8993(78)90568-1 · Cited by 1,220

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Lidstone, S. C., de la Fuente‐Fernández, R., & Stoessl, A. J. (2005) · Seminars in Pain Medicine · doi:10.1016/j.spmd.2005.02.004 · Cited by 35

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Echo, J. A., Lamonte, N., Christian, G., Znamensky, V., Ackerman, T. F., & Bodnar, R. J. (2001) · Brain Research · doi:10.1016/s0006-8993(01)03094-3 · Cited by 33

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Leung, B. K., Laurent, V., & Balleine, B. W. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-15754-7.00067-5 · Cited by 5

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Perry, M. L., Andrzejewski, M. E., Bushek, S. M., & Baldo, B. A. (2010) · Behavioral Neuroscience · doi:10.1037/a0018283 · Cited by 6

Voluntary wheel running effects on intra-accumbens opioid driven diet preferences in male and female rats

Lee, J. R., Tapia, M. A., Weise, V. N., Bathe, E. L., Vieira‐Potter, V. J., Booth, F. W., & Will, M. J. (2019) · Neuropharmacology · doi:10.1016/j.neuropharm.2019.05.017 · Cited by 6

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Huerta, C., Caba, M., & Camacho‐Morales, A. (2023) · Neuroscience · doi:10.1016/j.neuroscience.2023.08.019 · Cited by 8

Differential alcohol drinking behaviour and dependence in the Naples low- and high-excitability rat lines☆

Pellicano, M., & Sadile, A. G. (2006) · Behavioural Brain Research · doi:10.1016/j.bbr.2006.03.041 · Cited by 5

Substance and Behavioral Addictions Assessment Instruments

Grigsby, T. J. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.012 · Cited by 6

Specific Reaction Patterns to Distinct Positive Emotional Cues Related to Incentive Motivation in Dependence of the Taq1A-Polymorphism: Molecular Genetic Associations of Early and Late Event-Related Potentials

Munk, A. J. L., Wielpuetz, C., Osinsky, R., Müller, E. M., Grant, P. S., & Hennig, J. (2016) · Neuropsychobiology · doi:10.1159/000441658 · Cited by 5

Aversive Sensation in the Brain after Eating Unpalatable Food.

Manabe, Y., & Fushiki, T. (2002) · Journal of Nutritional Science and Vitaminology · doi:10.3177/jnsv.48.81 · Cited by 5

Endogenous opioid receptors and the feast or famine of maladaptive feeding

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Peciña, S., & Berridge, K. C. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.2329-05.2005 · Cited by 671

Increased food intake after opioid microinjections into nucleus accumbens and ventral tegmental area of rat

Mucha, R. F., & Iversen, S. D. (1986) · Brain Research · doi:10.1016/0006-8993(86)90622-0 · Cited by 159

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